Dexamethasone-loaded zeolitic imidazolate frameworks nanocomposite hydrogel with antibacterial and anti-inflammatory effects for periodontitis treatment.
Dexamethasone-loaded zeolitic imidazolate frameworks nanocomposite hydrogel with antibacterial and anti-inflammatory effects for periodontitis treatment.
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负载地塞米松沸石咪唑酯框架纳米复合水凝胶具有抗菌和抗炎作用,用于牙周炎治疗
DOI:
10.1016/j.mtbio.2022.100360
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发表时间:
2022-12
影响因子:
8.2
通讯作者:
Jiang, Liting
中科院分区:
文献类型:
--
作者:
Li, Ning;Xie, Lianyan;Wu, Yicheng;Wu, Yan;Liu, Yongjia;Gao, Yiming;Yang, Jie;Zhang, Xiuyin;Jiang, Liting
关键词:
Periodontitis is a bacterial-induced, chronic inflammatory disease characterized by progressive destruction of tooth-supporting structures. Pathogenic bacteria residing in deep periodontal pockets after traditional manual debridement can still lead to local inflammatory microenvironment, which remains a challenging problem and an urgent need for better therapeutic strategies. Here, we integrated the advantages of metal-organic frameworks (MOFs) and hydrogels to prepare an injectable nanocomposite hydrogel by incorporating dexamethasone-loaded zeolitic imidazolate frameworks-8 (DZIF) nanoparticles into the photocrosslinking matrix of methacrylic polyphosphoester (PPEMA) and methacrylic gelatin (GelMA). The injectable hydrogel could be easily injected into deep periodontal pockets, achieving high local concentrations without leading to antibiotic resistance. The nanocomposite hydrogel had high antibacterial activity and constructs with stable microenvironments maintain cell viability, proliferation, spreading, as well as osteogenesis, and down-regulated inflammatory genes expression in vitro. When evaluated on an experimental periodontitis rat model, micro-computed tomography and histological analyses showed that the nanocomposite hydrogel effectively reduced periodontal inflammation and attenuated inflammation-induced bone loss in a rat model of periodontitis. These findings suggest that the nanocomposite hydrogel might be a promising therapeutic candidate for treating periodontal disease.
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DOI:
10.3390/ma11101802
发表时间:
2018-09-22
期刊:
Materials (Basel, Switzerland)
影响因子:
--
作者:
Lasserre JF;Brecx MC;Toma S
通讯作者:
Toma S
影响因子:
3.7
作者:
Abranches J;Zeng L;Kajfasz JK;Palmer SR;Chakraborty B;Wen ZT;Richards VP;Brady LJ;Lemos JA
通讯作者:
Lemos JA
影响因子:
14
作者:
Jiang, Liting;Zhang, Wenjie;Jiang, Xinquan
通讯作者:
Jiang, Xinquan
影响因子:
6.7
作者:
Guo, Yu-Feng;Fang, Wei-Jun;Wang, Chun-Chang
通讯作者:
Wang, Chun-Chang
影响因子:
15.5
作者:
Galimanas V;Hall MW;Singh N;Lynch MD;Goldberg M;Tenenbaum H;Cvitkovitch DG;Neufeld JD;Senadheera DB
通讯作者:
Senadheera DB